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Dr Vivienne Miller

Based on an interview with Associate Professor Kirsten Black and Clinical Associate Professor Deborah Bateson conducted at the Annual Women’s and Children’s Health Update, Sydney in February 2018. "Heavy menstrual bleeding" is the new term for menorrhagia. This under-treated condition is easy to screen for in general practice. And screening for it is important as, apart from the discomfort, inconvenience, disturbed sleep, embarrassment and expense heavy menstrual bleeding causes, it is a major cause of iron deficiency in women. Common causes of heavy menstrual bleeding include hormonal variations relating to menarche and menopause, polycystic ovarian syndrome, polyps, fibroids and coagulation disorders. Identifying heavy menstrual bleeding initially involves discussing menstrual patterns with patients, as the diagnosis relies on the subjective experience of the woman as it affects her physical, emotional, social and/or material quality of life. Women may be unsure whether their periods are abnormally heavy compared with other women.  Questions that may assist in the diagnosis of  heavy menstrual bleeding include asking whether a woman needs to wear both a pad and a tampon simultaneously to prevent leakage, whether she has to use super pads and/or tampons and needs to change them every three hours or less, , whether she is concerned about flooding or staining during the day and avoids social activities as a result, whether she regularly takes time off work at the time of her period, whether she has to get up several times overnight to change her pad or tampon, whether she frequently passes clots (often this is associated with significant period pain), and finally, how the issue is affecting her quality of life. It is also important to inquire about associated symptoms such as pain, bloating and feelings of pressure on the bladder or bowel.Investigations usually include iron studies, a full blood count and a pelvic ultrasound. Ideally the ultrasound should be transvaginal as well as transabdominal. Also, ideally the ultrasound should be conducted between days five to 10 of the menstrual cycle, as this is when the uterine lining is less echogenic and scanning at this time reduces the chance of missing lesions such as polyps, within the uterine cavity. It should be noted that heavy menstrual bleeding may be a symptom of malignancy, especially in women over the age of 45 years. Other more specialised tests may also be indicated, such as coagulation studies, if there is suggestion of a bleeding diathesis. Once malignancy has been excluded as a cause of the bleeding, management usually includes hormonal control of the ovulation cycle, such as with the combined oral contraceptives. These reduce bleeding by 30%. An excellent alternative is the hormonal intrauterine system (Mirena®). If the woman prefers not to use such methods and is not at risk of pregnancy, tranexamic acid or norethisterone, 5mg three times daily, from days five to 26 of the menstrual cycle, can be used. NSAIDS such as mefenamic acid are most effective if commenced just prior to the onset of bleeding and continued into the first few days. Surgical management of heavy menstrual bleeding is usually indicated for women who have completed their families. The less invasive options include endometrial ablation and embolisation of fibroids. Hysterectomy is generally reserved for women in whom less invasive treatments have been unsuccessful, where there is a particular indication (such as large fibroids causing pressure symptoms) or less commonly, at the woman’s request.

Sophie Cousins

Mark King has had the clap so many times he’s renamed it ‘the applause’. The first time King had gonorrhoea, he was a teenager in the late 1970s, growing up with his five siblings in Louisiana. He had the telltale signs: burning and discomfort when he urinated and a thick discharge that left a stain in his underwear. King visited a clinic and gave a fake name and phone number. He was treated quickly with antibiotics and sent on his way. A few years later, the same symptoms reappeared. By this time, the 22-year-old was living in West Hollywood, hoping to launch his acting career. While King had come out to his parents, being gay in Louisiana was poles apart from being gay in Los Angeles. For one, homosexuality was illegal in Louisiana until 2003, whereas California had legalised it in 1976. In Los Angeles there was a thriving a gay scene where King, for the first time, could embrace his sexuality freely. He frequented bathhouses and also met men in dance clubs and along the bustling sidewalks. There was lots of sex to be had. “The fact that we weren’t a fully formed culture beyond those spaces… was what brought us together as people. Sex was the only expression we had to claim ourselves as LGBT people,” King says. When he stepped into the brick clinic just a few strides away from the heart of the city’s gay nightlife in Santa Monica, King, with his thick sandy blond hair with a tinge of red through it, looked around the room. It was filled with other gay men. “What do you do when you’re 22 and gay? You cruise other men. I remember sitting in the lobby cruising other men,” King recalls, laughing. “My Summer of Love was 1982. It was a playground. I was young and on the prowl.” Like a few years earlier, the doctor gave him a handful of antibiotics to take for a few days that would clear up the infection. It wasn’t a big deal. In fact, as King describes it, it was “simply an errand to run”. “It was the price of doing business and it wasn’t a high price at all.” But it was the calm before the storm, in more ways than one. When King picked up gonorrhoea again in the 1990s, he was greatly relieved that treatment was now just one dose. Penicillin was no longer effective, but ciprofloxacin was now the recommended treatment and it required only one dose. In King’s eyes, getting gonorrhoea was even less of a hassle. But this was actually a symptom of treatment regimens starting to fail. The bacteria Neisseria gonorrhoeae was on the way to developing resistance to nearly every drug ever used to treat it.

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Newsletter: On receiving the 1945 Nobel Prize in Physiology or Medicine for discovering penicillin, Alexander Fleming finished his lecture with a warning: “There is the danger,” he told the audience, “that the ignorant man may easily underdose himself and, by exposing his microbes to non-lethal quantities of the drug, make them resistant.” In other words, we have known about bacteria’s ability to evolve resistance to drugs since the dawn of the antibiotic era. Dr Manica Balasegaram is Director of the Global Antibiotic Research and Development Partnership (GARDP), based in Geneva. It’s a joint initiative between the Drugs for Neglected Diseases Initiative (DNDi) and the World Health Organization (WHO) and aims to develop new or improved treatments for bacterial infections. “All antibiotics will have a shelf life – that’s just evolution,” he says. “It’s just a question of how quickly it will happen.” Antibiotic resistance is one of the biggest threats to global health, food security and development. Common infections, such as pneumonia and tuberculosis, are becoming increasingly difficult to treat. But GARDP has chosen to focus its attention on gonorrhoea as one of its four main priorities. The sexually transmitted infection caught Balasegaram’s eyes for a host of reasons. For one, a lot of the antibiotics that are currently used against gonorrhoea are used widely for other infections, and N. gonorrhoeae has the ability to acquire resistance from other bacteria frighteningly quickly, meaning it can rapidly build up resistance. Secondly, untreated gonorrhoea infections bring with them a range of potentially serious health implications that can have devastating consequences. “Gonorrhoea is the most important sexually transmitted infection; it’s the one we’re most concerned about,” Balasegaram says. Every year an estimated 78 million people are infected with gonorrhoea, making it the second most frequently reported sexually transmitted bacterial infection after chlamydia, according to WHO. Gonorrhoea can infect the genitals, rectum and throat. Symptoms include discharge from the urethra or vagina and burning during urination called urethritis, caused by inflammation of the urethra. However, many who are infected don’t experience any symptoms, meaning they go undiagnosed and untreated. Complications of untreated gonorrhoea can be severe and disproportionately affect women, who are more likely to experience no symptoms. Untreated gonorrhoea not only increases the risk of contracting HIV but is also linked with an increased risk of pelvic inflammatory disease, which can cause ectopic pregnancy and infertility. A pregnant woman can also pass on the infection to her baby, which can cause blindness. Fixing the threat of resistant gonorrhoea won’t be easy – the challenges in developing a new antibiotic can’t be overestimated. Is the money for research and development (R&D) available? Who will the antibiotic be available to? And most importantly, how will you control its use so you can extend its shelf life? What makes the search for a new antibiotic for gonorrhoea particularly challenging is the frequency of asymptomatic infections along with gonorrhoea’s ability to adapt to its host’s immune system and develop resistance to antibiotics. A major concern is that because N. gonorrhoeae can live in the throat without someone even knowing, the bug can acquire resistance from other bacteria that also live there and which have been exposed to antibiotics in the past. And with evidence that oral sex is becoming increasingly common in some parts of the world, this is particularly challenging. “Oral sex is driving resistance. It’s a network of people having lots of oral sex. It’s the new norm,” says Dr Teodora Wi, a medical officer in WHO’s Department of Reproductive Health and Research in Geneva, talking specifically about Asia. These challenges and concerns have gripped Balasegaram, but nonetheless he’s more determined than ever to bring a new drug to market. “People are dying from drug-resistant infections. This is undoubtedly because this area has not been prioritised in the past because other areas of R&D are far more lucrative,” he says. “Antibiotics are a global public good. I don’t think it’s easy to put a financial value to it.”

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Recent data collected by WHO examined trends in drug-resistant gonorrhoea in 77 countries – countries that are part of the health agency’s Gonococcal Antimicrobial Surveillance Programme (GASP), a global network of regional and subregional laboratories that track the emergence and spread of resistance. And the results are grim. More than 80 per cent of the countries that reported on azithromycin, a commonly prescribed antibiotic used to treat numerous common infections, including sexually transmitted infections (STIs), found resistance. Of greatest concern is that 66 per cent of countries surveyed have reported cases that resist last-resort antibiotics called extended-spectrum cephalosporins (ESCs). And as Wi points out, the real-world picture is undoubtedly far bleaker, because global surveillance for drug-resistant gonorrhoea is patchy and more frequently done in higher-income countries, which have greater resources. For example, of the 77 countries that were surveyed, few were in sub-Saharan Africa, a region where rates of gonorrhoea are high. “We’re only seeing half of the real picture. We need to prepare for the future when there’s no cure,” Wi says. But in a sign that time is running out, in March this year health experts’ worst fears were confirmed: a case of super-gonorrhoea, dubbed the world’s “worst ever” case, was found in a man who had attended a local sexual health clinic. He had reportedly had sexual contact with a woman in South-east Asia. Health officials said it was the first time this strain could not be cured with any of the antibiotics normally used to treat the disease. Although the patient has since responded to another antibiotic, doctors described him as “very lucky”. It’s an indication of a wider crisis – and one that knows no boundaries.

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Thailand is one country on the front line of the fight against antibiotic-resistant gonorrhoea. It’s a key destination for the sex tourism industry, where STIs like gonorrhoea can spread easily and quickly across borders and beyond. And like many other countries in the region, it has an over-the-counter culture of antibiotic access, which means patients put themselves at risk of being prescribed the wrong drugs – or even worse. I’m in a district close to Thailand’s capital, Bangkok, to meet Boontham, a pharmacist. We meet in the jam-packed stockroom of the herbal medicine company he also runs – a business that’s far more lucrative than his pharmacy. The stockroom is filled head to toe with boxes of tablets containing an array of funky herbs I’ve never heard of. The cost of visiting a doctor and the stigma surrounding STIs mean that many Thais rely on pharmacists like Boontham to cure their gonorrhoea. But he might be doing more harm than good. While Boontham has a degree in pharmacology and has been a pharmacist for more than 30 years, he has no idea of Thailand’s treatment guidelines for gonorrhoea. In fact, he’s more than a decade out of date. And he can’t, of course, diagnose patients accurately, particularly because gonorrhoea has similar symptoms to chlamydia. “If you’ve been doing this for a long time, you just do what you have to, and that’s an educated guess.” “As of now I use ciprofloxacin [to treat gonorrhoea],” he says. “If that doesn’t work, then I guess it’s chlamydia.” I tell him, however, that gonorrhoea in Thailand, as in many other countries, has shown widespread resistance to ciprofloxacin – and that his country actually stopped recommending it more than a decade ago. “It’s not resistant, even doctors use it,” he says. “I prescribe it because it’s cheap. In hospitals they prescribe newer antibiotics that are more effective, but they’re more expensive.” In countries where antibiotics are sold over the counter, research shows people are far more likely to visit pharmacists than a doctor. But while experts acknowledge that restricting the sale of antibiotics – particularly in rural and remote areas where there are few, if any, proper doctors – isn’t the answer, this still presents a major challenge in the fight against drug-resistant infections. “The problem is that when you go to a pharmacist and take antibiotics, maybe… your symptoms have disappeared, but in fact you still have the infection. That means you can transmit the infection and cause more resistance,” Wi says. I ask Boontham whether he’s concerned about resistance – if he’s worried that the people he’s treated for gonorrhoea aren’t cured. “Resistance to medication is a doctor’s job, not a pharmacist’s,” he says. The casual handing out of antibiotics without a prescription is not only confined to Thailand. It’s a huge concern across the rest of the region and in other parts of the world, with no clear vision of how to tackle this growing problem. Handing out antibiotics that likely no longer work for people with gonorrhoea has also been happening in high-income countries – countries that might be expected to have stricter treatment guidelines. In fact, a study published in the BMJ in 2015 found that many GPs in England were prescribing ciprofloxacin, even though it hasn’t been recommended for treating gonorrhoea since 2005. In 2007, ciprofloxacin still made up almost half of prescriptions for gonorrhoea. As recently as 2011, GPs still prescribed it in 20 per cent of cases.

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On a balmy afternoon in bustling Bangkok, I visit Silom Community Clinic @ TropMed, an STI clinic north-east of the city centre dedicated to men who have sex with men (MSM) and transgender women who have sex with men. Located on the 12th floor of the Hospital for Tropical Diseases, the clinic is spotlessly clean, with bright purple walls, rainbow flags and a sign that immediately catches my eye, which reads “Suck, F*ck, Test, Repeat”. Off the main corridor is a microbiology lab that is doing critical and urgent work in the fight against antibiotic-resistant gonorrhoea. In fact, the lab may be the best way Thailand can protect itself from this growing threat. Dr Eileen Dunne is an American epidemiologist and the head of the behavioural and clinical research section of the HIV/STI programme here, which is run as part of a collaboration between Thailand’s Ministry of Public Health (MOPH) and the US Centers for Disease Control and Prevention (CDC). She, along with her Thai staff, are Thailand’s best line of defence in slowing gonorrhoea resistance. In 2015, recognising the worldwide danger of increasingly difficult to treat gonorrhoea infections – and the specific threat they posed to Thailand – the US CDC, WHO and Thai MOPH joined forces to launch a programme to track and ultimately limit the spread of antibiotic-resistant gonorrhoea. The programme is an enhanced local version of the WHO’s GASP and is the first of its kind in the world. It’s called EGASP. It works like this. If a male patient comes into one of its two clinics with the telltale symptoms of gonorrhoea, he will have a sample collected for analysis and will fill out a questionnaire, which contains questions such as: “Did you take antibiotics in the last two weeks?” To create an open environment, the clinics are anonymous and the questionnaire is done privately on a computer. Men are the target group in the programme, Dunne explains, because the yield for isolating N. gonorrhoeae is very high among men who have urethritis compared with women and those who are asymptomatic. MSM are an important population, she adds, because research shows they are likelier to develop resistance earlier than the general population, for reasons that aren’t precisely known. She and the laboratory staff take me to see if there are any samples being cultured from swabs taken from patients’ penises. Inside the incubator, where the samples are kept in Petri dishes at 36 degrees Celsius with 5 per cent carbon dioxide to promote bacteria growth, there are three. The stench of agar, a brown gelatinous medium that provides nutrients and a stable environment for bacteria to grow, is overwhelming. One Petri dish contains a cluster of bubbly white dots, signalling that the patient does indeed have gonorrhoea. The next step is antibiotic susceptibility testing (AST) at a lab downstairs. The isolate will be measured for resistance to five antibiotics, including ciprofloxacin and the last-resort drugs cefixime and ceftriaxone. It’s resistance to these latter two which is of greatest concern. From the beginning of EGASP until 20 October 2017, of the 845 confirmed diagnoses of gonorrhoea that underwent AST, almost all isolates had widespread resistance to ciprofloxacin, as in many other countries. But encouragingly, none have shown resistance to the last-line drugs. That’s a relief for Thailand, but in no way an indication that Dunne and her team’s alacrity should wane. “People are surprised and have asked, ‘Oh, why are you doing this if you don’t show resistance?’,” Dunne says. “It’s actually good to do surveillance and not be detecting resistance yet. It means that we’re early enough to be prepared… and [to] have a plan of response. “Having strong surveillance activity in a region in which this is likely to emerge is important so we can detect it early.” Thailand’s neighbours, specifically Myanmar, India, Indonesia and China, have recorded a significantly higher percentage of gonorrhoea isolates that are resistant to last-line treatments compared to Thailand. With the increasing movement of people around the world and Thailand’s popularity for sex tourism, I can see just how rapidly this threat could have far-reaching consequences. “I think it’s really important to detect early, even one case, [because] it can be a harbinger for future developments of resistance. These bacteria are transmitted very rapidly between people. Being able to really find that one case early means that special steps can be in place to control transmission,” Dunne says. I ask if the focus on MSM means other groups might be being missed. What about women, who are more likely than men to not experience any gonorrhoea symptoms? Or itinerant sex workers from across the border in Myanmar and Cambodia? I wonder if, among this high-risk group, EGASP is missing some of Thailand’s most vulnerable. I ask if there’s potential for the programme to extend its work to include these people and their partners. Dunne agrees it’s a good idea. “This targeted approach in men with symptoms is purposeful but may not be generalisable to the whole population. It’s the tip of the iceberg.” But it’s early on in the programme, and she and the team have to start somewhere. “We need more time,” she says. But no one is really sure how much time Thailand – and the rest of the world – has.

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The number of people infected with gonorrhoea has risen rapidly in recent years. Australia has seen a 63 per cent increase in the number of reported gonorrhoea cases since 2012, with the fastest rate of increase being in young heterosexual urbanites. In England, gonorrhoea cases rose by 53 per cent between 2012 and 2015, led by young people, gay men and other MSM. Meanwhile, in the USA cases rose by nearly 50 per cent between 2009 and 2016. And according to some experts, one of science’s greatest achievements in the fight against HIV could be a factor. Like many, Mark King’s nonchalant attitude towards sex had come to a halt when the HIV epidemic hit the gay community in the USA. No longer was gonorrhoea simply seen as a small, insignificant price to pay for a night of fun. “Half the fun of being gay [was that] you didn’t have to worry about birth control. Condoms were birth control, not STI control,” says King. “[But] as the years passed and you get into the 90s and we know how HIV is transmitted, to get gonorrhoea is shameful because it means that you’ve been taking risks that could transmit HIV. “Suddenly gonorrhoea became this really shameful thing because it means you’re not doing the right thing.” Move forward to today and HIV is no longer the death threat it once was. A strong civil society movement saw the disease get the political – and scientific – attention it warranted. The development of life-saving drugs means that those with HIV can live long, healthy lives. But as HIV treatment and prevention methods improve, people’s perception of risk may be changing. Pre-exposure prophylaxis (PrEP) is a daily pill for people who don’t have HIV but who are at substantial risk of getting it. It’s a powerful tool in the fight against HIV, it is argued. When taken every day, it’s up to 92 per cent effective in preventing infection. But with its development and uptake came alarm bells, with some warning that STI rates would increase among those who used PrEP. Some small studies have hinted that this may be happening. Not all experts agree with this. The data from these studies is ambiguous and cannot be generalised. And some say that regular testing regimes associated with PrEP prescriptions could prevent STIs spreading. However, just as with antibiotics, there are people using PrEP without getting it through official health outlets. A recent survey carried out across Europe by the HIV/AIDS advocacy group AIDES found that about 70 per cent of informal PrEP users were having no regular medical monitoring. King is one of many for whom concerns over STIs in the broader context of having the incredible ability to prevent HIV infection seems absurd. “PrEP opens the door for people to have sex without fear of HIV infection. The reaction is: yes, but what do we do about STIs? Oh my god, gonorrhoea and syphilis,” King says sarcastically. “People ask me, how does a person get HIV or gonorrhoea in this day and age? Well, let’s see: because they were horny, or they said yes when they should have said no, or they had too much to drink, or they fell in love, or they trusted the wrong person.” King’s words may resonate with many around the world. But WHO is focused on increasing condom use. Wi is particularly worried about the proliferation and popularity of dating apps among young people, which she believes are making no-strings-attached sex easier to obtain. “All of us need to be strong about condom use. All of us need to campaign for condom use,” Wi says.

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Looking ahead, at what point will it be more common to have a gonorrhoea infection that can’t be treated with antibiotics than one that can? The answer is difficult to predict, but it’s also a potential reality that isn’t far-fetched. “We are in a situation now where we are worryingly using the last line of antibiotics for many infections or seeing even resistance to these last-line antibiotics,” Balasegaram says. But as GARDP works to bring a new antibiotic to market, some countries are getting desperate as resistance to the available treatments continues to spread. Australia, which has recorded widespread resistance to azithromycin, is considering going back to an old drug called spectinomycin. Spectinomycin involves a painful muscular injection and has been linked to toxicity and a range of side-effects. Another concern is that it’s in short supply because it’s rarely used around the world any more. To this end, R&D for new antibiotics is urgent. But antibiotic drug development is prohibitively expensive and not attractive to the pharmaceutical industry – even more so when it’s for an STI. In response, GARDP has partnered with Entasis Therapeutics, a US biotech company, to accelerate the development of a new antibiotic that will be produced specifically to target drug-resistant gonorrhoea. Zoliflodacin is a novel first-in-class oral antibiotic – in other words, a new and unique mechanism of potentially treating gonorrhoea – and is one of only three potential new antibiotic candidates currently undergoing trials. It had previously been put through clinical trials in 2015, but a lack of investment stopped the drug from progressing further. This year GARDP and Entasis will launch the last phase of trials of zoliflodacin, involving 650 people in Thailand, South Africa, the USA and parts of Europe. If the drug is approved by regulators, Entasis will permit GARDP to introduce it in 168 low- and middle-income countries. It’s hoping it will be registered by 2021 and available on the market by 2023. A major strength of the partnership between GARDP and Entasis is that it will be able to limit what infections zoliflodacin is used for. “We’re trying to focus this drug specifically on STIs – not other community infections where antibiotics are widely used,” Balasegaram says. “The aim is not to go beyond that because that’s how resistance starts.” To this end, initially the drug will be licensed only for use against gonorrhoea infections. If it proves to be effective against chlamydia and Mycoplasma genitalium (another bacterial STI), the GARDP and Entasis partnership could license it for those two infections as well, subject to clinical trials. “We will support clinical trials and registration and therefore we can play a big role in how it is responsibly introduced and used. That gives us more control in how the drug is introduced and marketed in the countries where we work,” says Balasegaram. Dunne is excited that Thailand will be part of the trials. “It is the underbelly of infections. It doesn’t get the attention it deserves and that is why this is exciting,” she says. A lot is riding on the success of the drug. Will zoliflodacin be successful in remaining effective for as long as possible? Or will it face the same fate as other antibiotics? Moreover, research is risky – there’s no guarantee the clinical trials will be successful. “We still don’t know whether this project will succeed or not,” says Balasegaram. “But it’s a project that we feel is extremely important and that we’re very committed to.” The development of new antibiotics raises myriad questions: How can we ensure they are used appropriately so we can preserve their effectiveness? And how can we ensure those who really need the drugs get them? One way would be a point-of-care rapid diagnostic test – ideally one that could predict which antibiotics will work on a particular infection and that could be used in settings around the world. Balasegaram says they’ve been looking for a simple diagnostic tool like this but haven’t yet found one. Diagnostic tools aside, the responsible use of new antibiotics also relies on robust national and international treatment guidelines and strong regulatory authorities to guide and monitor antibiotic use. “If you have developed an antibiotic for narrow use, you have to think about how to market the drug. We do not want to drop large quantities of it around the world. But we also want to make sure those who need it get it,” he says. This is where strong surveillance programmes, like Thailand’s, are critical. But it’s inevitable that bugs will develop resistance to the next antibiotic and then the next. So Balasegaram wants more investment in R&D that focuses not only on new antibiotics but also on alternative ways to treat bacterial infections. “We have to continue to do R&D into… therapeutic ways to treat these infections differently,” he says. “This may include novel and non-conventional approaches. I think that is a job that is going to last decades.” What that might look like is complex. It may include designing antibodies that specifically target bacteria or using bacteriophages – viruses that infect bacteria – as a replacement for antibiotics. Either way, many feel that the end of the antibiotic era is near and that the transition from antibiotics to non-traditional treatments poses major challenges that won’t be easy to solve. “It’s worth bearing in mind that bacteria can evolve to different approaches we develop,” says Balasegaram. “I don’t think we will see a magic bullet solution soon that will definitively solve the issue.” It’s a frightening thought. Mark King has had the clap so many times he’s renamed it ‘the applause’. The first time King had gonorrhoea, he was a teenager in the late 1970s, growing up with his five siblings in Louisiana. He had the telltale signs: burning and discomfort when he urinated and a thick discharge that left a stain in his underwear. King visited a clinic and gave a fake name and phone number. He was treated quickly with antibiotics and sent on his way. A few years later, the same symptoms reappeared. By this time, the 22-year-old was living in West Hollywood, hoping to launch his acting career. While King had come out to his parents, being gay in Louisiana was poles apart from being gay in Los Angeles. For one, homosexuality was illegal in Louisiana until 2003, whereas California had legalised it in 1976. In Los Angeles there was a thriving a gay scene where King, for the first time, could embrace his sexuality freely. He frequented bathhouses and also met men in dance clubs and along the bustling sidewalks. There was lots of sex to be had. “The fact that we weren’t a fully formed culture beyond those spaces… was what brought us together as people. Sex was the only expression we had to claim ourselves as LGBT people,” King says. When he stepped into the brick clinic just a few strides away from the heart of the city’s gay nightlife in Santa Monica, King, with his thick sandy blond hair with a tinge of red through it, looked around the room. It was filled with other gay men. “What do you do when you’re 22 and gay? You cruise other men. I remember sitting in the lobby cruising other men,” King recalls, laughing. “My Summer of Love was 1982. It was a playground. I was young and on the prowl.” Like a few years earlier, the doctor gave him a handful of antibiotics to take for a few days that would clear up the infection. It wasn’t a big deal. In fact, as King describes it, it was “simply an errand to run”. “It was the price of doing business and it wasn’t a high price at all.” But it was the calm before the storm, in more ways than one. When King picked up gonorrhoea again in the 1990s, he was greatly relieved that treatment was now just one dose. Penicillin was no longer effective, but ciprofloxacin was now the recommended treatment and it required only one dose. In King’s eyes, getting gonorrhoea was even less of a hassle. But this was actually a symptom of treatment regimens starting to fail. The bacteria Neisseria gonorrhoeae was on the way to developing resistance to nearly every drug ever used to treat it.

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Recent data collected by WHO examined trends in drug-resistant gonorrhoea in 77 countries – countries that are part of the health agency’s Gonococcal Antimicrobial Surveillance Programme (GASP), a global network of regional and subregional laboratories that track the emergence and spread of resistance. And the results are grim. More than 80 per cent of the countries that reported on azithromycin, a commonly prescribed antibiotic used to treat numerous common infections, including sexually transmitted infections (STIs), found resistance. Of greatest concern is that 66 per cent of countries surveyed have reported cases that resist last-resort antibiotics called extended-spectrum cephalosporins (ESCs). And as Wi points out, the real-world picture is undoubtedly far bleaker, because global surveillance for drug-resistant gonorrhoea is patchy and more frequently done in higher-income countries, which have greater resources. For example, of the 77 countries that were surveyed, few were in sub-Saharan Africa, a region where rates of gonorrhoea are high. “We’re only seeing half of the real picture. We need to prepare for the future when there’s no cure,” Wi says. But in a sign that time is running out, in March this year health experts’ worst fears were confirmed: a case of super-gonorrhoea, dubbed the world’s “worst ever” case, was found in a man who had attended a local sexual health clinic. He had reportedly had sexual contact with a woman in South-east Asia. Health officials said it was the first time this strain could not be cured with any of the antibiotics normally used to treat the disease. Although the patient has since responded to another antibiotic, doctors described him as “very lucky”. It’s an indication of a wider crisis – and one that knows no boundaries.

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Thailand is one country on the front line of the fight against antibiotic-resistant gonorrhoea. It’s a key destination for the sex tourism industry, where STIs like gonorrhoea can spread easily and quickly across borders and beyond. And like many other countries in the region, it has an over-the-counter culture of antibiotic access, which means patients put themselves at risk of being prescribed the wrong drugs – or even worse. I’m in a district close to Thailand’s capital, Bangkok, to meet Boontham, a pharmacist. We meet in the jam-packed stockroom of the herbal medicine company he also runs – a business that’s far more lucrative than his pharmacy. The stockroom is filled head to toe with boxes of tablets containing an array of funky herbs I’ve never heard of. The cost of visiting a doctor and the stigma surrounding STIs mean that many Thais rely on pharmacists like Boontham to cure their gonorrhoea. But he might be doing more harm than good. While Boontham has a degree in pharmacology and has been a pharmacist for more than 30 years, he has no idea of Thailand’s treatment guidelines for gonorrhoea. In fact, he’s more than a decade out of date. And he can’t, of course, diagnose patients accurately, particularly because gonorrhoea has similar symptoms to chlamydia. “If you’ve been doing this for a long time, you just do what you have to, and that’s an educated guess.” “As of now I use ciprofloxacin [to treat gonorrhoea],” he says. “If that doesn’t work, then I guess it’s chlamydia.” I tell him, however, that gonorrhoea in Thailand, as in many other countries, has shown widespread resistance to ciprofloxacin – and that his country actually stopped recommending it more than a decade ago. “It’s not resistant, even doctors use it,” he says. “I prescribe it because it’s cheap. In hospitals they prescribe newer antibiotics that are more effective, but they’re more expensive.” In countries where antibiotics are sold over the counter, research shows people are far more likely to visit pharmacists than a doctor. But while experts acknowledge that restricting the sale of antibiotics – particularly in rural and remote areas where there are few, if any, proper doctors – isn’t the answer, this still presents a major challenge in the fight against drug-resistant infections. “The problem is that when you go to a pharmacist and take antibiotics, maybe… your symptoms have disappeared, but in fact you still have the infection. That means you can transmit the infection and cause more resistance,” Wi says. I ask Boontham whether he’s concerned about resistance – if he’s worried that the people he’s treated for gonorrhoea aren’t cured. “Resistance to medication is a doctor’s job, not a pharmacist’s,” he says. The casual handing out of antibiotics without a prescription is not only confined to Thailand. It’s a huge concern across the rest of the region and in other parts of the world, with no clear vision of how to tackle this growing problem. Handing out antibiotics that likely no longer work for people with gonorrhoea has also been happening in high-income countries – countries that might be expected to have stricter treatment guidelines. In fact, a study published in the BMJ in 2015 found that many GPs in England were prescribing ciprofloxacin, even though it hasn’t been recommended for treating gonorrhoea since 2005. In 2007, ciprofloxacin still made up almost half of prescriptions for gonorrhoea. As recently as 2011, GPs still prescribed it in 20 per cent of cases.

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On a balmy afternoon in bustling Bangkok, I visit Silom Community Clinic @ TropMed, an STI clinic north-east of the city centre dedicated to men who have sex with men (MSM) and transgender women who have sex with men. Located on the 12th floor of the Hospital for Tropical Diseases, the clinic is spotlessly clean, with bright purple walls, rainbow flags and a sign that immediately catches my eye, which reads “Suck, F*ck, Test, Repeat”. Off the main corridor is a microbiology lab that is doing critical and urgent work in the fight against antibiotic-resistant gonorrhoea. In fact, the lab may be the best way Thailand can protect itself from this growing threat. Dr Eileen Dunne is an American epidemiologist and the head of the behavioural and clinical research section of the HIV/STI programme here, which is run as part of a collaboration between Thailand’s Ministry of Public Health (MOPH) and the US Centers for Disease Control and Prevention (CDC). She, along with her Thai staff, are Thailand’s best line of defence in slowing gonorrhoea resistance. In 2015, recognising the worldwide danger of increasingly difficult to treat gonorrhoea infections – and the specific threat they posed to Thailand – the US CDC, WHO and Thai MOPH joined forces to launch a programme to track and ultimately limit the spread of antibiotic-resistant gonorrhoea. The programme is an enhanced local version of the WHO’s GASP and is the first of its kind in the world. It’s called EGASP. It works like this. If a male patient comes into one of its two clinics with the telltale symptoms of gonorrhoea, he will have a sample collected for analysis and will fill out a questionnaire, which contains questions such as: “Did you take antibiotics in the last two weeks?” To create an open environment, the clinics are anonymous and the questionnaire is done privately on a computer. Men are the target group in the programme, Dunne explains, because the yield for isolating N. gonorrhoeae is very high among men who have urethritis compared with women and those who are asymptomatic. MSM are an important population, she adds, because research shows they are likelier to develop resistance earlier than the general population, for reasons that aren’t precisely known. She and the laboratory staff take me to see if there are any samples being cultured from swabs taken from patients’ penises. Inside the incubator, where the samples are kept in Petri dishes at 36 degrees Celsius with 5 per cent carbon dioxide to promote bacteria growth, there are three. The stench of agar, a brown gelatinous medium that provides nutrients and a stable environment for bacteria to grow, is overwhelming. One Petri dish contains a cluster of bubbly white dots, signalling that the patient does indeed have gonorrhoea. The next step is antibiotic susceptibility testing (AST) at a lab downstairs. The isolate will be measured for resistance to five antibiotics, including ciprofloxacin and the last-resort drugs cefixime and ceftriaxone. It’s resistance to these latter two which is of greatest concern. From the beginning of EGASP until 20 October 2017, of the 845 confirmed diagnoses of gonorrhoea that underwent AST, almost all isolates had widespread resistance to ciprofloxacin, as in many other countries. But encouragingly, none have shown resistance to the last-line drugs. That’s a relief for Thailand, but in no way an indication that Dunne and her team’s alacrity should wane. “People are surprised and have asked, ‘Oh, why are you doing this if you don’t show resistance?’,” Dunne says. “It’s actually good to do surveillance and not be detecting resistance yet. It means that we’re early enough to be prepared… and [to] have a plan of response. “Having strong surveillance activity in a region in which this is likely to emerge is important so we can detect it early.” Thailand’s neighbours, specifically Myanmar, India, Indonesia and China, have recorded a significantly higher percentage of gonorrhoea isolates that are resistant to last-line treatments compared to Thailand. With the increasing movement of people around the world and Thailand’s popularity for sex tourism, I can see just how rapidly this threat could have far-reaching consequences. “I think it’s really important to detect early, even one case, [because] it can be a harbinger for future developments of resistance. These bacteria are transmitted very rapidly between people. Being able to really find that one case early means that special steps can be in place to control transmission,” Dunne says. I ask if the focus on MSM means other groups might be being missed. What about women, who are more likely than men to not experience any gonorrhoea symptoms? Or itinerant sex workers from across the border in Myanmar and Cambodia? I wonder if, among this high-risk group, EGASP is missing some of Thailand’s most vulnerable. I ask if there’s potential for the programme to extend its work to include these people and their partners. Dunne agrees it’s a good idea. “This targeted approach in men with symptoms is purposeful but may not be generalisable to the whole population. It’s the tip of the iceberg.” But it’s early on in the programme, and she and the team have to start somewhere. “We need more time,” she says. But no one is really sure how much time Thailand – and the rest of the world – has.

§

The number of people infected with gonorrhoea has risen rapidly in recent years. Australia has seen a 63 per cent increase in the number of reported gonorrhoea cases since 2012, with the fastest rate of increase being in young heterosexual urbanites. In England, gonorrhoea cases rose by 53 per cent between 2012 and 2015, led by young people, gay men and other MSM. Meanwhile, in the USA cases rose by nearly 50 per cent between 2009 and 2016. And according to some experts, one of science’s greatest achievements in the fight against HIV could be a factor. Like many, Mark King’s nonchalant attitude towards sex had come to a halt when the HIV epidemic hit the gay community in the USA. No longer was gonorrhoea simply seen as a small, insignificant price to pay for a night of fun. “Half the fun of being gay [was that] you didn’t have to worry about birth control. Condoms were birth control, not STI control,” says King. “[But] as the years passed and you get into the 90s and we know how HIV is transmitted, to get gonorrhoea is shameful because it means that you’ve been taking risks that could transmit HIV. “Suddenly gonorrhoea became this really shameful thing because it means you’re not doing the right thing.” Move forward to today and HIV is no longer the death threat it once was. A strong civil society movement saw the disease get the political – and scientific – attention it warranted. The development of life-saving drugs means that those with HIV can live long, healthy lives. But as HIV treatment and prevention methods improve, people’s perception of risk may be changing. Pre-exposure prophylaxis (PrEP) is a daily pill for people who don’t have HIV but who are at substantial risk of getting it. It’s a powerful tool in the fight against HIV, it is argued. When taken every day, it’s up to 92 per cent effective in preventing infection. But with its development and uptake came alarm bells, with some warning that STI rates would increase among those who used PrEP. Some small studies have hinted that this may be happening. Not all experts agree with this. The data from these studies is ambiguous and cannot be generalised. And some say that regular testing regimes associated with PrEP prescriptions could prevent STIs spreading. However, just as with antibiotics, there are people using PrEP without getting it through official health outlets. A recent survey carried out across Europe by the HIV/AIDS advocacy group AIDES found that about 70 per cent of informal PrEP users were having no regular medical monitoring. King is one of many for whom concerns over STIs in the broader context of having the incredible ability to prevent HIV infection seems absurd. “PrEP opens the door for people to have sex without fear of HIV infection. The reaction is: yes, but what do we do about STIs? Oh my god, gonorrhoea and syphilis,” King says sarcastically. “People ask me, how does a person get HIV or gonorrhoea in this day and age? Well, let’s see: because they were horny, or they said yes when they should have said no, or they had too much to drink, or they fell in love, or they trusted the wrong person.” King’s words may resonate with many around the world. But WHO is focused on increasing condom use. Wi is particularly worried about the proliferation and popularity of dating apps among young people, which she believes are making no-strings-attached sex easier to obtain. “All of us need to be strong about condom use. All of us need to campaign for condom use,” Wi says.

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Looking ahead, at what point will it be more common to have a gonorrhoea infection that can’t be treated with antibiotics than one that can? The answer is difficult to predict, but it’s also a potential reality that isn’t far-fetched. “We are in a situation now where we are worryingly using the last line of antibiotics for many infections or seeing even resistance to these last-line antibiotics,” Balasegaram says. But as GARDP works to bring a new antibiotic to market, some countries are getting desperate as resistance to the available treatments continues to spread. Australia, which has recorded widespread resistance to azithromycin, is considering going back to an old drug called spectinomycin. Spectinomycin involves a painful muscular injection and has been linked to toxicity and a range of side-effects. Another concern is that it’s in short supply because it’s rarely used around the world any more. To this end, R&D for new antibiotics is urgent. But antibiotic drug development is prohibitively expensive and not attractive to the pharmaceutical industry – even more so when it’s for an STI. In response, GARDP has partnered with Entasis Therapeutics, a US biotech company, to accelerate the development of a new antibiotic that will be produced specifically to target drug-resistant gonorrhoea. Zoliflodacin is a novel first-in-class oral antibiotic – in other words, a new and unique mechanism of potentially treating gonorrhoea – and is one of only three potential new antibiotic candidates currently undergoing trials. It had previously been put through clinical trials in 2015, but a lack of investment stopped the drug from progressing further. This year GARDP and Entasis will launch the last phase of trials of zoliflodacin, involving 650 people in Thailand, South Africa, the USA and parts of Europe. If the drug is approved by regulators, Entasis will permit GARDP to introduce it in 168 low- and middle-income countries. It’s hoping it will be registered by 2021 and available on the market by 2023. A major strength of the partnership between GARDP and Entasis is that it will be able to limit what infections zoliflodacin is used for. “We’re trying to focus this drug specifically on STIs – not other community infections where antibiotics are widely used,” Balasegaram says. “The aim is not to go beyond that because that’s how resistance starts.” To this end, initially the drug will be licensed only for use against gonorrhoea infections. If it proves to be effective against chlamydia and Mycoplasma genitalium (another bacterial STI), the GARDP and Entasis partnership could license it for those two infections as well, subject to clinical trials. “We will support clinical trials and registration and therefore we can play a big role in how it is responsibly introduced and used. That gives us more control in how the drug is introduced and marketed in the countries where we work,” says Balasegaram. Dunne is excited that Thailand will be part of the trials. “It is the underbelly of infections. It doesn’t get the attention it deserves and that is why this is exciting,” she says. A lot is riding on the success of the drug. Will zoliflodacin be successful in remaining effective for as long as possible? Or will it face the same fate as other antibiotics? Moreover, research is risky – there’s no guarantee the clinical trials will be successful. “We still don’t know whether this project will succeed or not,” says Balasegaram. “But it’s a project that we feel is extremely important and that we’re very committed to.” The development of new antibiotics raises myriad questions: How can we ensure they are used appropriately so we can preserve their effectiveness? And how can we ensure those who really need the drugs get them? One way would be a point-of-care rapid diagnostic test – ideally one that could predict which antibiotics will work on a particular infection and that could be used in settings around the world. Balasegaram says they’ve been looking for a simple diagnostic tool like this but haven’t yet found one. Diagnostic tools aside, the responsible use of new antibiotics also relies on robust national and international treatment guidelines and strong regulatory authorities to guide and monitor antibiotic use. “If you have developed an antibiotic for narrow use, you have to think about how to market the drug. We do not want to drop large quantities of it around the world. But we also want to make sure those who need it get it,” he says. This is where strong surveillance programmes, like Thailand’s, are critical. But it’s inevitable that bugs will develop resistance to the next antibiotic and then the next. So Balasegaram wants more investment in R&D that focuses not only on new antibiotics but also on alternative ways to treat bacterial infections. “We have to continue to do R&D into… therapeutic ways to treat these infections differently,” he says. “This may include novel and non-conventional approaches. I think that is a job that is going to last decades.” What that might look like is complex. It may include designing antibodies that specifically target bacteria or using bacteriophages – viruses that infect bacteria – as a replacement for antibiotics. Either way, many feel that the end of the antibiotic era is near and that the transition from antibiotics to non-traditional treatments poses major challenges that won’t be easy to solve. “It’s worth bearing in mind that bacteria can evolve to different approaches we develop,” says Balasegaram. “I don’t think we will see a magic bullet solution soon that will definitively solve the issue.” It’s a frightening thought. This article first appeared on Mosaic and is republished here under a Creative Commons licence.

Dr Vivienne Miller

Based on an interview with Sydney dermatologist, Dr Rob Rosen conducted at the Annual Women’s and Children’s Health Update, Sydney in February 2018. Hyperhidrosis is a very distressing condition that equally affects both men and women, across all ethnicities.  It occurs in approximately 3% of the general population and the onset is in childhood or adolescence. However, only about one third of people affected seek medical advice. In addition to the physical effects, the psychological impact on affected individuals is significant. Embarrassment, anxiety and depression are very commonly associated with this condition. In primary hyperhidrosis, the sweat glands are normal but there is an apparently exaggerated sympathetic response. The sweat glands most susceptible to these sympathetic cholinergic effects are the eccrine glands found in the palms, soles and axillae. Primary, focal hyperhidrosis tends to be bilateral and symmetrical, occurring at least once a week. It usually commences before a person reaches their mid-twenties and is often familial.  In its typical form, and if there is nothing to suggest a secondary cause, it requires no investigations. Secondary hyperhidrosis is typically generalised, affecting the entire surface of the skin. By definition, it has an underlying cause, such as infection, endocrine disturbance, neuropathy, malignancy, menopause, drug withdrawal or the side-effect of medications.  A full history, examination and targeted investigations are required before this condition can be called idiopathic. “It is important to make the distinction between “generalised” and “focal” hyperhidrosis at the outset,” says Sydney dermatologist, Dr Rob Rosen The management of hyperhidrosis begins conservatively. By the time they present to a doctor they usually have already tried a range of antiperspirants.  Aluminium hydroxide 20%, topically, daily for four weeks should be trialled before further treatment is considered. Many patients develop localised irritation to this treatment, as it obstructs the eccrine ducts, causing their atrophy. The most effective management is Botulinum A toxin injections. This drug blocks the release of acetylcholine from presynaptic nerve terminals, thus inhibiting the stimulation of the eccrine sweat gland. The injections are done intradermally and retreatment is needed approximately every six months. Over time, this duration between treatments may become longer. Side effects include discomfort at the injection site and, less commonly, weakness of local muscles (especially relating to small muscles in the hand, for example, in palmer hyperhidrosis). In the research done by Dr Rosen t al, over 90% of patients were happy with this therapy.1 Oral anticholinergics such as oxybutynin (5mg to 15mg daily) or glycopyrrolate (1mg to 4mg daily) may be used and are most effective in refractory cases of generalised sweating. The anticholinergic side effects (urinary retention, dry mouth, constipation) tend to be a limiting factor in their use. Other treatments for hyperhidrosis tend to be either less effective or more invasive. For patients over 12 years old, there is a Medicare rebate for Botulinum A injection therapy for severe primary axillary hyperhidrosis, if aluminium hydroxide has failed and if it is administered by a dermatologist, neurologist or paediatrician. Some cosmetic clinics treat patients without a rebate and this is often a more expensive option.
  1. Rosen R, Stewart T. Results of a 10-year follow-up study of botulinum toxin A therapy for primary axillary hyperhidrosis in Australia. Intern Med J; 48;343-347.

Dr David Palmer

The importance of eosinophils and neutrophils infiltrating oesophageal squamous epithelium as markers for reflux, eosinophilic oesophagitis, and infection are well entrenched, although traditionally less attention has been paid to lymphocytes. Small numbers of lymphocytes are normally seen in oesophageal epithelium including CD4 helper and CD8 positive cytotoxic lymphocytes. However, isolated increases in lymphocytes in the oesophageal epithelium, outside the context of entities such as lichen planus and graft versus host disease, have been less well recognised until recently. The criteria for a diagnosis of lymphocytic oesophagitis, where lymphocyte numbers are markedly increased with few or no eosinophils, is not strictly defined since this is still a reaction pattern and not a specific diagnosis per se, and thresholds vary from study to study. The strictest definition requires at least 50 intraepithelial or peripapillary lymphocytes per HPF with few or no granulocytes. The term lymphocytic oesophagitis was originally coined in 2005 by Rubio et al to describe a histological reaction pattern in the oesophagus of a series of 20 patients. The patients had a high number of peripapillary lymphocytes and a lack of neutrophils and eosinophils. The papillae are projections of lamina propria, containing capillaries, which project a short distance into the epithelium of the normal oesophagus. The pattern of lymphocytic oesophagitis showed an association with Crohn’s disease, though not a completely specific one. Of the 20 patients, 11 were age 17 or younger and of these, eight (40%) had Crohn’s disease; 20% had manifestations of reflux and the remainder a mixture of conditions including coeliac, gastroduodenitis, and Hashimoto’s thyroiditis. A similar study of 40 patients in 2008 was unable to confirm these findings. Looking at it from a different angle, Ebach et al studied 60 paediatric patients with known Crohn’s disease and control groups and found an association. Lymphocytic oesophagitis  which was found in 28% of patients with Crohn’s disease (mean age 13.3) but in only 2/30 patients with ulcerative colitis. A 2014 study of 580 paediatric patients confirms the association with Crohn’s disease, but also shows the non-specific nature of lymphocytic oesophagitis. This found 31 patients with lymphocytic oesophagitis and 49 with Crohn’s disease. Six of the 31 lymphocytic oesophagitis patients (19%) and 43 of the 514 non- lymphocytic oesophagitis patients (8.4%) had Crohn’s disease. The remaining lymphocytic oesophagitis patients had other diagnoses with no significant clinical correlates. Conversely, lymphocytic oesophagitis was identified in 12.2% of the patients with Crohn’s disease. Thus, there were still more lymphocytic oesophagitis patients without Crohn’s disease than with Crohn’s disease. In adults, the association with Crohn’s disease is not seen but there appears to be an association with oesophageal dysmotility. A 2011 study of over 129,000 patients from a large outpatient private GI pathology lab service revealed lymphocytic oesophagitis in only 119 patients, 60% female. Most patients had symptoms of oesophageal disease such as dysphagia or odynophagia, with dysphagia being the most common complaint, and around 20% complaining of reflux. Endoscopically, around a third of patients were suspected of having eosinophilic oesophagitis (including ‘feline oesophagus’ where the oesophagus has rings resembling that of a cat’s oesophagus), around 20% were normal, 18% had features suggestive of reflux, and 10% had stricture. However, none had Crohn’s disease or an association with Helicobacter gastritis. Although this study drew no firm conclusions as to the nature of lymphocytic oesophagitis in adults, the prevalence of dysphagia as a presenting complaint, and the number of patients with findings reminiscent of eosinophilic oesophagitis were noted. The association with dysmotility is enhanced by the finding that in adult patients, a lymphocytic oesophagitis with a complete absence of granulocytes was mostly seen in older female patients who presented with dysphagia and had an oesophageal motility disorder. CD4- and CD8-predominant lymphocytic oesophagitis occurs with roughly equal frequency. However, patients with CD4-predominant lymphocytic oesophagitis are more likely to be female (71%), and have a motility disorder (90% of those tested). This suggests a new entity of ‘dysmotility lymphocytic oesophagitis’. In summary, the reaction pattern of lymphocytic oesophagitis appears to be real, however, the term cannot be used as a wastebasket and true increased numbers of intraepithelial lymphocytes must be seen. Clinical and endoscopic correlations determine the significance of any pathologist comment on increased numbers of lymphocytes in the epithelium.
General Practice Pathology is a new regular column each authored by an Australian expert pathologist on a topic of particular relevance and interest to practising GPs. The authors provide this editorial, free of charge as part of an educational initiative developed and coordinated by Sonic Pathology.

Suzanne Dyer

A new study out today has found residents with dementia in aged-care facilities that provide a home-like model of care have a better quality of life and fewer hospitalisations than those living in more standard facilities. We also found the benefits of a home-like model were provided without an increase in running costs. Our study compared home-like models (which have up to 15 residents per unit and free access to outdoor areas) to more standard residential care, where a large number of people are housed in one building. In 2011, around half of all facilities in Australia had places for more than 60 residents, and the average size is growing. The World Health Organisation has stated smaller home-like residential care settings “hold promise for older people, family members and volunteers who provide care and support”. But Australia is lagging behind other countries in offering alternative models of residential aged care.
Read more: There's no need to lock older people into nursing homes 'for their own safety'

What is a home-like model of care?

Most older people with dementia want to stay at home as long as they can. When this is no longer possible, they move into residential aged-care facilities, which become their homes. These residential facilities, or nursing homes, frequently adopt a model of care that emphasises individuality. This is known as person-centred care. But delivering this model may require more staff or a different mix of staff, which may be difficult to deliver with current funding. So standard aged-care facilities in Australia often have some similarities to health facilities, with designated staff areas and centralised kitchens. Access to outdoor areas, particularly for people with dementia, may depend on the availability of staff. Despite adhering to philosophies such as person-centred care, the scheduling of this care and of meals often lacks flexibility. The problems are compounded when residential care is used for multiple purposes ranging from palliative care to providing care for people with dementia. The needs of these two groups are quite different and the lack of focus makes delivering quality care a challenge. Evidence shows the physical design of the residential aged-care environment may play an important role in the well-being of residents, particularly those living with dementia. Internationally, there is a move towards providing care in facilities that feel more like a home and promote independence. Such models of residential aged care generally have:
  • flexibility in daily routines – for example, the time people get dressed and eat
  • opportunity for residents to participate in domestic activities such as meal preparation
  • access to outdoor spaces
  • clusters of smaller living units (up to, say, 15 residents in each)
  • care staff assigned to living units for continuity of care and development of relationships between staff and residents.

Read more: God’s waiting room? Life needs to be valued in nursing homes

What we found

Our study was specifically designed to include people with dementia and their family members. People with dementia are not often included in research studies. It included 541 participants from 17 not-for-profit residential aged-care facilities in four different states in Australia. They had been residents for a year or longer. These facilities were all considered high quality. This means they had lower hospitalisation rates for potentially avoidable conditions than the national performance target. And more than 80% of residents in the standard care facilities indicated they felt as safe as they wanted and that their environment was as clean and comfortable as they wanted. Around one-quarter of people in the study lived in a facility with a home-like model of care. All of them were living with dementia. The study found residents in home-like models of care had a better quality of life, as rated by the residents themselves or their family members. They also had a 68% lower rate of being admitted to hospital and 73% lower rate of having an emergency department presentation. We have previously shown residents who lived in a home-like model were 52% less likely to be exposed to potentially inappropriate medications. These are medications where the potential harms may outweigh the benefit, such as antipsychotics or relaxants, but are still often prescribed to older people in residential care. The benefits for residents were provided with similar running costs for the home-like and the standard models of care. However, the costs excluded differences in the build of the facilities. Initial establishment costs are likely to be higher, due to the requirement for more space per resident.
Read more: There is extra funding for aged care in the budget, but not enough to meet demand

Rethinking models of care

Funding arrangements don’t incentivise Australian aged-care providers to offer variety in terms of models of care. Government funding is provided based on the assessed care needs of the residents, rather than the preferred model of care or resident outcomes. Funding supplements are available to care providers for reasons such as residents’ financial hardship or risk of homelessness and to small, rural aged-care service providers, but none are available for offering an alternative model of care. The ConversationThe Australian government plans to improve the aged-care system to offer “choice and flexibility”. This is crucial, but we also need to improve choice and variety in residential aged-care models. Suzanne Dyer, Senior Research Fellow, Flinders University and Stephanie Harrison, Postdoctoral research fellow, Flinders University This article was originally published on The Conversation. Read the original article.
Dr Vivienne Miller

Based on an interview with Melbourne urologist, Dr Caroline Dowling conducted in March, 2018 Australia was the first country to ban vaginal mesh products used surgically via transvaginal implantation for the treatment of pelvic organ prolapse. Australia was also a leader in evaluating the complications of these implant, through large scale research.1 On November 28th 2017, the Therapeutic Goods Administration withdrew implants for use in prolapse, stating it “was of the belief that the benefits of using transvaginal mesh products in the treatment of pelvic organ prolapse do not outweigh the risks these products pose to patients”. There are unique risks related to mesh use. These include mesh erosion (up to 14% of cases)1, vaginal and groin pain (up to 3% to 4%)1 and mesh exposure. These complications may be more common and more severe (requiring surgery) if the mesh is used for prolapse repair, as opposed to the treatment of stress incontinence. Reports of complications associated with transvaginal mesh products began over a decade, with the Food and Drug Administration issuing an alert about their use back in 2008. Repeated warnings were then given. In 2013, legal action began in Australia with 300 women registering for a national class action against Johnson & Johnson Medical Australia. So what do GPs tell their patients who have a vaginal mesh in situ, and what alternative managements are there for vaginal prolapse and stress incontinence? Patients who feel they have complications should be reviewed by the surgeon who operated on them, but it worth noting that most women have had no problems with these products and so, in the absence of symptoms may be reassured that they need no further management. “Women who have no problems from their transvaginal mesh implants should be reassured that they do not require them to be removed,” says Melbourne urologist Dr Caroline Dowling There is not an inherent risk with mesh as an implant, it is used widely in general surgery for inguinal hernia and abdominal wound repair. Nonetheless, it would be wise to explain the possible side-effects of the vaginal mesh in case these occur in the future. Alternatives to the vaginal mesh implant are the traditional vaginal prolapse repair using native tissue, and these are effective procedures for most women seeking surgical treatment of their prolapse. There are several alternatives to mesh for the treatment of stress incontinence that has failed conservative therapy, including an autologous fascial sling, bulking agents and Burch colposuspension. In 2015, the Cochrane Incontinence Group concluded that mid-urethral slings were highly effective in the short-term and medium-term and had a good safety profile. The mid-urethral sling remains available in its retropubic and transobturator form, but patients can no longer access mini-slings or single incision slings outside trial settings. This may change once the results of longer term studies become available. Single incisions may have a more favourable side-effect profile than full-length slings. More conservative management includes pelvic floor exercises and silicon pessaries inserted for prolapse and stress incontinence treatment. Pelvic floor exercises may be difficult to do effectively and repeatedly for many women, especially over time. They may also be less effective in cases of significant cystocoele. Silicon pessaries are particularly useful in women who are symptomatic but wish to have further pregnancies, in women who do not want surgery, in the elderly and for those in poor health.3 Patients may need help with the insertion and correct placement, but pessaries work well and may be an underutilised option.
  1. A/Prof. Christopher Maher, Explaining the Vaginal Mesh Controversy. Royal Brisbane and Women's and Wesley Hospitals Brisbane, The University of Queensland. June 17th
https://medicine.uq.edu.au/article/2017/06/explaining-vaginal-mesh-controversy
  1. Ford et al. Mid-urethral sling operations for stress urinary incontinence in women. Cochrane Incontinence Group, July 2015.
http://cochranelibrary-wiley.com/doi/10.1002/14651858.CD006375.pub3/abstract
  1. Jones, K. Harmanli, O. Pessary Use in Pelvic Organ Prolapse and Urinary Incontinence. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2876320

Dr Linda Calabresi

Surviving childhood cancer is a major win in anyone’s language. However, it is well-known, that even as adults these survivors are at an increased risk of dying before the age of their cancer-history-free peers. Now, it would appear, these people can do something about managing that Damocles sword. According to a recent study published in JAMA Oncology, regular vigorous exercise in early adulthood is associated with a lower risk of mortality in adult survivors of childhood cancer. And the study authors believe the finding could have a significant impact, given the numbers of children that now survive cancer. “These findings may be of importance for the large and rapidly growing population of adult survivors of childhood cancer at substantially higher risk of mortality due to multiple competing risks,” they said. The study was a multicentre cohort analysis of data from over 15,400 adults who had had cancer diagnosed at one of number of paediatric tertiary hospitals in North America before the age of 21. Interviews were conducted at baseline (median age at almost 26 years) at which, among a range of other parameters, levels of exercise were assessed. These patients were then followed for up to 15 years (median follow-up 9.6 years). Overall, after adjusting for chronic health conditions and treatment exposures the researchers found an inverse association between exercise and all-cause mortality. More compelling was the analysis of a subset of almost 5700 survivors, which showed that increased exercise over an eight-year period was associated with a 40% reduction in all-cause mortality compared with low levels of exercise. Of course, the critical question is what constitutes vigorous or increased exercise? How much exercise does a person need to do to qualify for this benefit? The question these patients were asked was ‘on how many of the past seven days did you exercise or do a sport that made you sweat or breathe hard?’ This was considered vigorous exercise, and the mortality benefit was seen in people who exercised to this level for at least 60 minutes a week. But the benefit was not entirely dose-dependent.  It appeared that vigorously exercising for about an hour a day, five days a week (eg a brisk 60 min walk) was the most advantageous in terms of mortality, beyond that the benefit was attenuated. It is well known that, in the general population, regular exercise reduces all-cause and cause-specific mortality, however there are much fewer studies looking at its benefit among cancer survivors, especially younger-age cancer survivors. “To this end, our findings….significantly extend the current evidence base and arguably provide the best available epidemiological evidence to support the endorsement of exercise for cancer survivors,” the study authors said. Ref: JAMA Oncology doi10:1001/jamaoncol.2018.2254

Dr Trevor W. Beer

Melanoma is rare in childhood, representing no more than 2% of all skin melanomas. Diagnosis is often delayed because melanoma is unsuspected, partly due to differences in presentation and its rarity. The diagnosis is made with trepidation by pathologists, since the vast majority of childhood skin lesions are benign. Establishing the true prevalence of juvenile melanoma is complicated by a number of factors, one being the definition of childhood or juvenile. Many studies use a cut-off age of 19 years, but this is not consistent. Cancer registry data may also be unreliable due to misclassified Spitz naevi, for example.

ABCDE + ABCDD

ABCDE criteria help to identify adult melanoma clinically (Asymmetry, Border irregularity, Colour variation, Diameter >6mm, Evolution). Many melanomas in childhood are non-pigmented (> 50% of 65 recent cases from Victoria). Additional ABCD criteria have been suggested in children: Amelanotic, Bleeding bump, Colour uniformity, De novo, any Diameter to facilitate earlier recognition. Children more often present with advanced disease due to diagnostic delay, reported in 50-60% of patients.

Childhood Melanoma in WA

A recent WA study with the WA Melanoma Advisory Service (WAMAS) identified 95 melanomas in patients 19 years or younger over a 14-year period. Three patients died from melanoma. The majority of tumours, 75%, occurred between ages 13 and 19 years, similar to other studies. In all populations, juvenile melanoma is much less common before puberty. Delayed diagnosis was evident with 21 of 23 patients presenting with Clark level 4 or 5 melanomas with Breslow thickness >1mm in 65%. A family history of melanoma was seen in 17%. A study this year in Victoria revealed 65 melanomas during a 19-year period, with seven fatalities. A decrease in juvenile melanoma has been seen in WA despite an increasing population. In Queensland, a substantial decline occurred between 1997 and 2010, attributed to safer sun exposure practices since the 1980s.

Prognosis

The outlook for childhood melanoma mirrors that in adults being primarily based on stage and Breslow thickness. The exceptions are tumours with spitzoid features. These show appearances resembling Spitz naevi and, although often metastasising to local nodes, are less frequently lethal. Prognostication is complicated by the fact that occasional examples behave aggressively and some spitzoid melanomas in case series may be misdiagnosed Spitz naevi.

Treatment

Complete excision, as in adults, is required. Further investigations and treatment should be decided in conjunction with expert advice. Treatment of advanced melanoma is progressing rapidly and possible eligibility for clinical trials means that patients will get the best opportunities for positive outcomes with personally tailored, up-to-date guidance. It is recommended that all melanoma diagnoses in childhood are reviewed by pathologists with expertise in melanocytic lesions. Referral to a multidisciplinary team is valuable to ensure correct diagnosis and to optimise treatment and advice to patients and families.

Sophie Spitz’s ‘Juvenile Melanoma’

Pathologist Sophie Spitz described 12 unusual ‘juvenile melanomas’ in 1948. Follow-up showed benign behaviour, despite microscopy suggesting melanoma. These lesions are now called Spitz naevi. Although typically childhood lesions, they can occur in adults, reducing in frequency with age. Diagnosis clinically and microscopically can be challenging. Lesions may clinically resemble pyogenic granulomas, haemangioma or dermatofibroma. While most are correctly identified pathologically, some are misdiagnosed as melanoma. Conversely, a leading cause of litigation in pathology is underdiagnosis of melanoma as Spitz naevus. Distinction between Spitz naevi and melanoma may be extremely difficult or even impossible. In these histologically ambiguous tumours inter-observer agreement is notoriously poor. There is now a move away from traditional benign versus malignant divisions with suggestions that a histological continuum exists between Spitz naevi at one end and Spitzoid melanoma at the other. Indeterminate lesions may be labelled Spitzoid tumours of uncertain malignant potential (STUMP) with a guarded prognosis.

Improving pathological diagnostic accuracy

Treatment and prognostication of childhood melanoma requires accurate diagnosis which can be enhanced by experience and consultation between pathologists. Molecular studies such as FISH and aCGH may assist in ambiguous cases, but such methods are still in development and not uniformly available. However, molecular techniques will ultimately lead to more accurate diagnosis, prognostication and tailored treatment for children with melanoma. References available on request
General Practice Pathology is a new regular column each authored by an Australian expert pathologist on a topic of particular relevance and interest to practising GPs. The authors provide this editorial, free of charge as part of an educational initiative developed and coordinated by Sonic Pathology.
Dr Linda Calabresi

Almost three quarters of men with low grade prostate cancer may not be being adequately monitored, a recent Victorian study suggests. According to data from the Prostate Cancer Outcomes Registry – Victoria, only 26.5% of over 1600 men who had low risk prostate cancer had follow-up investigations consistent with standard active surveillance protocols in the two years after their diagnosis. Specifically, researchers were investigating whether these men adhered to the schedule that consisted of at least three PSA measures and at least one biopsy in the two years post diagnosis. While the study authors concede the clinical consequences of this shortcoming are yet unknown, the finding is still of concern. “If [these men] are not being followed appropriately according to [Active Surveillance] protocols, men may miss the opportunity to be treated with curative intent,” they wrote in the MJA. Active surveillance is increasingly the management of choice for men with low risk prostate cancer. In Victoria, 60% of men diagnosed with this grade of cancer are now managed with active surveillance, the study authors said. A major issue with active surveillance as a management option, is that the optimal timing of follow-up investigations has not been strictly defined, resulting in several different protocols and guidelines being developed worldwide.  This, in part was the impetus for the development of the Victorian prostate cancer registry, which was established in 2009 ‘to improve knowledge of patterns of care and outcomes for men diagnosed with prostate cancer.’ Currently the Australian protocol for active surveillance is based on the consensus opinion, and the three PSA tests and repeat biopsy within two years has been widely accepted as standard care. The finding that 73.5% did not receive monitoring in accordance with thisprotocol, reflected adherence levels that were among the worst when compared to similar studies around the world, and the study authors suggested the reason was likely to be multifactorial. The reasons for the non-compliance ‘may reflect patient-, clinician- and health service-related factors,” they wrote. Patients may avoid biopsy because of pain, clinicians may delay testing based on a patient’s comorbidities or health services may have fewer resources for sending reminders or pursuing patients who miss appointments, the study authors suggested. Nonetheless, efforts needed to be made to ensure men with low grade prostate cancer are not disadvantaged in terms of health outcomes if they opt to accept active surveillance as their management strategy. “To improve adherence, a multifaceted approach may be required, including an education campaign that highlights the need for men to undergo regular PSA assessment and prostate biopsy,” they concluded. Ref: MJA doi:10.5694/mja17.00559

Prof Adam Watkins

ON THE PILL: In this seven-part series we explore the history, myths, side-effects and alternatives of the pill, and why it’s the most popular form of contraception in Australia.
The female contraceptive pill has helped millions of women take control of their fertility and reproductive health since it became available in 1961. Yet a male equivalent has yet to be fully developed. This effectively leaves men with only two viable contraceptive options: condoms or a vasectomy. The idea of creating a male contraceptive has been around almost as long as the female contraceptive. In theory, targeting the production of sperm should be a simple process. The biology of sperm production and how they swim towards the egg are well understood. Yet, studies aimed at developing an effective male pill have been dogged by issues such as severe side effects. Most recently, a study that injected men with the hormones testosterone and progestogen – similar to hormones found in the female pill – had to be stopped early.
Read more: Why the male 'pill' is still so hard to swallow
The study, from 2016, showed pregnancy rates for female partners of men receiving the injections fell below that typically seen for women on the pill. But the study was cut short due to reports of adverse side effects including acne, mood disorders and raised libido. For the men taking part, these side effects proved too severe for them to continue, despite the desired drop in sperm production. However, many people may see these side effects as relatively minor compared to those suffered by women on the pill, which include anxiety, weight gain, nausea, headaches, reduced libido and blood clots. Male contraceptives have been under development for at least 50 years. However, the drive to bring a male contraceptive onto the market has stalled for two main reasons. First, there is a general pessimism of men towards taking a contraceptive pill, especially in countries such as India. Second, the global success of the female pill provides little incentive for pharmaceuticals to invest in a male pill. Globally, the female pill is the third most-used form of contraception, with a projected market value of nearly US$23 billion by 2023. Despite these setbacks, a new way of thinking about male contraception is taking shape. Here, the focus has shifted from stopping sperm production to stopping the sperm being able to fertilise the egg.

The clean sheet pill

The clean sheet pill effectively works as its name suggests: preventing the release of sperm. The clean sheet pill has two main selling points. First, by preventing the release of sperm and the fluid they are carried in, the clean sheet pill simultaneously prevents unwanted pregnancy and the spread of sexually-transmitted infections. Second, because the pill does not affect the feeling of orgasm, there is no reduction in male sexual pleasure. Unfortunately, the clean sheet pill has so far only been tested in animals. As such, a version for human use is probably ten years away from being developed.

Vasalgel

One of the downsides of a vasectomy is that it can render a man permanently sterile. However, the recent development of a product call Vasalgel may offer men a serious alternative to a vasectomy. Vasalgel is a long-term, non-hormonal yet reversible form of contraception. This offers benefits over both hormonal contraceptives with their side effects as well as the permanency of a vasectomy. Vasalgel is polymer that is injected into the vas deferens, the tube that carries sperm from the testes. This allows the movement of fluid, but stops the passage of sperm.
Read more: A new male contraceptive could help men bear the family planning burden
In a trial in monkeys, Vasagel was found to be 100% effective at preventing conception. In separate studies in animals, the effect of Vasagel was easily reversed with a simple second injection to dissolve the polymer. If these effects are replicated in men, this could offer a low-cost, minimally invasive and effective contraceptive that is also reversible.

Heart-stopping poisons

A deadly, heart-stopping poison might not sound like a good starting point for a new male contraceptive. However, researchers have shown that a toxic compound call oubain can be be used to slow down the swimming of sperm. Researchers already knew that oubain could affect male fertility. But the cardio toxic effects of oubain prevented scientists from exploring its effects on male reproduction in any detail. By modifying the structure of the oubain molecule, researchers showed it can be used to reduce the motility (ability to swim) of rat sperm while being non-toxic to the heart.

Research and development

While research into male contraceptives have been ongoing for nearly 50 years, we still seem to be at least “five to ten years away” from an effective male pill.
Read more: We won't have a male contraceptive until we change our understanding of risk
Potential new targets for male contraceptives are being developed and tested scientifically all the time. However, without the significant input and push from big pharmaceutical companies, these discoveries may never see the light of day. The ConversationWith the cost of developing a new drug to market estimated at US$2.6 billion, the burden of family planning looks to remain firmly on the shoulders of women for now. Adam Watkins, Assistant Professor, University of Nottingham This article was originally published on The Conversation. Read the original article.
Dr Linda Calabresi

In what will be seen as a blow to cryptic crossword compilers the world over, it appears wealth is a better determinant of whether you keep your marbles than education. In a UK prospective study of over 6000 adults aged over 65 years, researchers found those people in the lowest quintile in terms of socioeconomic status were almost 70% more likely to get dementia than those categorised to be in the top fifth, over a 12 year follow-up period. Depressingly, this finding held true regardless of education level. “This longitudinal cohort study found that wealth in late life, but not education, was associated with increased risk of dementia, suggesting people with fewer financial resources were at higher risk,” the study authors said. On further analysis, researchers found the association between wealth, or the lack thereof and dementia was even more pronounced in the younger participants in the cohort. So what did the researchers think was the reason behind the link between poverty and dementia? One explanation was that having money allowed one to access more mentally stimulating environments including cultural resources (reading, theatre etc) and increased social networks that might help preserve cognitive function. While on the flip side, poverty (or ‘persistent socioeconomic disadvantage’ as the authors describe it) affects physiological functioning, increasing the risk of depression, vascular disease and stroke – all known risk factors for dementia. Other factors such as poor diet and lack of exercise also appear to more common among poorer people in the community. All this seems fairly logical, but what of the lack of a protective effect of education? Well, the researchers think this might be a particularly British phenomenon in this age group. “This might be a specific cohort effect in the English population born and educated in the period surrounding the World War II,” they suggested. A number of other studies have shown other results, with some, including the well-respected Canadian Study of Health and Aging-  showing the complete opposite – education protects against dementia. Consequently, the authors of this study, published in JAMA Psychiatry, hypothesise that perhaps this cohort of patients may have been unable to access higher education because of military service or financial restrictions but were able to access intellectually challenging jobs after the war. All in all, the study is an observational one and it is possible there are a number of confounding factors from smoking to availability of medical care that play a role in why poorer people are at greater risk of dementia. And while the researchers are not advocating older people give up their Bridge game and just buy lottery tickets, it would seem money is useful, if not for happiness, then at least for preserving brain power. Ref: JAMA Psychiatry doi:10.1001/jamapsychiatry.2018.1012

Dr Paul Glendenning

Markers of bone turnover, measured in blood or urine, correlate with changes in the metabolic activity of bone. The rate of bone remodelling is important. With ageing, the quantum of bone removed/ resorbed and the amount replaced/ formed becomes increasingly imbalanced. Consequently, the more bone remodelling units that are active at any one time, or the greater the activity of individual units, the greater the overall rate of bone loss. Bone turnover markers are probably predictive of the rate of bone loss and could help determine the efficacy of treatment.

Bone turnover markers:

  • May predict fracture risk independently of bone mineral density, according to some studies.
  • A drop in bone resorption is an early predictor of response to all anti-resorptive osteoporosis treatments initiated in general practice (bisphosphonates, denosumab or raloxifene), with these markers changing earlier than comparable markers of bone formation.
  • They may be predictive of later changes in bone mineral density (BMD), and can be measured before BMD changes can be evaluated.

Which bone resorption marker?

Markers measuring the rate of bone loss are degradation products of type 1 collagen cleaved during bone resorption. Cross-linking telopeptides of collagen can be measured by immunoassays that are specific for the beginning (N terminal- called NTX) or end (C terminal- called CTX) of type 1 collagen. While measuring urinary NTX and serum CTX provide comparable information there are some advantages of CTX over NTX. Consequently, serum CTX has been proposed as a reference method. The measurand in the CTX assay is clearly defined, allowing this 8 amino acid oligopeptide to become the reference method.
  • Most serum CTX is from osteoclastic bone resorption (indicating high specificity).
  • The assay can be performed manually or by automated methods and is only provided by one manufacturer (obviating the need for harmonisation)
  • The biological and analytical variability for CTX is well documented in the literature.

Uses and limitations

Serum CTX is a potentially useful test when investigating the cause of increased alkaline phosphatase, verifying compliance with osteoporosis treatment, improving persistence with that treatment or identifying occult secondary causes of osteoporosis such as apathetic hyperthyroidism or other metabolic bone disorders such as Paget’s disease. Samples collected fasting in the morning minimise intra-individual variation and requests ideally should include the reason for testing. Medicare currently provides a rebate for tests of bone resorption in patients with known bone disease taking treatment.
  1. Not all anti-resorptive treatments suppress bone resorption to the same degree. Provision of the type of anti-resorptive agent used and the duration of treatment is not only helpful for billing but allows us to report more specifically - whether the rate of bone resorption is typical or higher than expected for a particular anti-resorptive agent. For example, denosumab suppresses bone resorption earlier and to a greater degree than a bisphosphonate.
  2. Bone resorption is not predictive of future fracture risk in individuals. CTX can provide complementary information to bone mineral density in subpopulations but this measurement has not been currently adopted into fracture risk alogrithm calculators such as FRAX or the Garvan risk calculator for individuals.
  3. The measurement of serum CTX cannot be used to select treatment. This is because the baseline rate of bone remodelling is not predictive of the rate of change of bone remodelling or rate of change of bone density while on treatment.
  4. Measurement of bone formation and bone resorption do not provide additive information. While bone remodelling is a coupled process wherein bone formation and bone resorption are linked, the measurement of bone resorption or bone formation markers provide comparable information regarding the rate of bone remodelling. Measurements of both bone formation and bone resorption markers in individual patients do not help determine the degree of imbalance in bone remodelling and is therefore unnecessary. Understanding these limitations and the potential value of measuring bone remodelling markers can be useful when making decisions regarding individual patient management in those taking treatment for osteoporosis.
Reproduced with permission from Medical Forum magazine Oct 2017 edition
General Practice Pathology is a new regular column each authored by an Australian expert pathologist on a topic of particular relevance and interest to practising GPs. The authors provide this editorial, free of charge as part of an educational initiative developed and coordinated by Sonic Pathology.